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Open access
volume 9 issue 39 pages 22313-22319

Ultra-small palladium nano-particles synthesized using bulky S/Se and N donor ligands as a stabilizer: application as catalysts for Suzuki–Miyaura coupling

Preeti Oswal 1, 2, 3, 4, 5, 6
Aayushi Arora 1
Jolly Kaushal 1, 2, 3, 4, 5, 6
Gyandshwar Kumar Rao 2, 7, 8, 9, 10, 11
Sushil Kumar 1, 2, 3, 4, 5, 6
Ajai Singh 2, 11, 12, 13, 14
Arun Kumar 1, 2, 3, 4, 5, 6
1
 
Department of Chemistry, School of Physical Sciences, Doon University, Dehradun, 248012 India
2
 
DEPARTMENT OF CHEMISTRY
3
 
School of Physical Sciences
4
 
Doon University
5
 
Dehradun
6
 
248012 India
8
 
Amity School of Applied Sciences
10
 
Gurgaon
11
 
INDIA
12
 
Department of Chemistry, India Institute of Technology Delhi, New Delhi, India
13
 
India Institute of Technology Delhi
14
 
NEW DELHI
Publication typeJournal Article
Publication date2019-07-18
scimago Q1
wos Q2
SJR0.777
CiteScore7.6
Impact factor4.6
ISSN20462069
PubMed ID:  35519491
General Chemistry
General Chemical Engineering
Abstract
Two chalcogenated ligands L1 and L2 containing anthracene core and amine functionality have been synthesized. Both the ligands have been characterized using 1H and 13C{1H} NMR techniques. The structure of L1 has also been corroborated by single crystal X-ray diffraction. Application of L1 and L2 as stabilizers for palladium nano-particles (NPs) has been explored and six different types of NPs 1-6 have been prepared by varying the quantity of stabilizer. The nano-particles have been characterized by PXRD, EDX, and HRTEM techniques. The size of NPs has been found to be in the range of ∼1-2 nm, 2-3 nm, 4-6 nm, 1-2 nm, 1-2 nm and 3-5 nm for 1-6 respectively. The catalytic activities of 1-6 have been explored for Suzuki-Miyaura coupling of phenyl boronic acid with various aryl halides. These NPs showed good catalytic activity for various aryl chlorides/bromides at low catalyst loading (5 mg). Among 1-6, the highest activity has been observed for NPs 1, probably due to their relatively small size and high uniformity in the dispersion. The recyclability of the NPs upto 5 catalytic cycles is a distinct advantage.
Found 
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GOST Copy
Oswal P. et al. Ultra-small palladium nano-particles synthesized using bulky S/Se and N donor ligands as a stabilizer: application as catalysts for Suzuki–Miyaura coupling // RSC Advances. 2019. Vol. 9. No. 39. pp. 22313-22319.
GOST all authors (up to 50) Copy
Oswal P., Arora A., Kaushal J., Rao G. K., Kumar S., Singh A., Kumar A. Ultra-small palladium nano-particles synthesized using bulky S/Se and N donor ligands as a stabilizer: application as catalysts for Suzuki–Miyaura coupling // RSC Advances. 2019. Vol. 9. No. 39. pp. 22313-22319.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1039/c9ra03498f
UR - https://xlink.rsc.org/?DOI=C9RA03498F
TI - Ultra-small palladium nano-particles synthesized using bulky S/Se and N donor ligands as a stabilizer: application as catalysts for Suzuki–Miyaura coupling
T2 - RSC Advances
AU - Oswal, Preeti
AU - Arora, Aayushi
AU - Kaushal, Jolly
AU - Rao, Gyandshwar Kumar
AU - Kumar, Sushil
AU - Singh, Ajai
AU - Kumar, Arun
PY - 2019
DA - 2019/07/18
PB - Royal Society of Chemistry (RSC)
SP - 22313-22319
IS - 39
VL - 9
PMID - 35519491
SN - 2046-2069
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2019_Oswal,
author = {Preeti Oswal and Aayushi Arora and Jolly Kaushal and Gyandshwar Kumar Rao and Sushil Kumar and Ajai Singh and Arun Kumar},
title = {Ultra-small palladium nano-particles synthesized using bulky S/Se and N donor ligands as a stabilizer: application as catalysts for Suzuki–Miyaura coupling},
journal = {RSC Advances},
year = {2019},
volume = {9},
publisher = {Royal Society of Chemistry (RSC)},
month = {jul},
url = {https://xlink.rsc.org/?DOI=C9RA03498F},
number = {39},
pages = {22313--22319},
doi = {10.1039/c9ra03498f}
}
MLA
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Oswal, Preeti, et al. “Ultra-small palladium nano-particles synthesized using bulky S/Se and N donor ligands as a stabilizer: application as catalysts for Suzuki–Miyaura coupling.” RSC Advances, vol. 9, no. 39, Jul. 2019, pp. 22313-22319. https://xlink.rsc.org/?DOI=C9RA03498F.
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